FDA Inspection 1081930 — KEDPlasma LLC
The FDA completed an inspection of KEDPlasma LLC on Feb 27, 2019 in Youngstown, OH. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Feb 27, 2019
- Fiscal Year
- 2019
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Youngstown, OH (United States)